<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li D</submitter><funding>Natural Science Foundation of Hubei Province</funding><funding>National Natural Science Foundation of China</funding><pagination>2791-2795</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6419947</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(9)</volume><pubmed_abstract>Electrochemical oxidative C-H/S-H cross-coupling has been developed to construct the C-S bond in a highly straightforward and efficient manner. Various enamines and (hetero)aryl thiols could be transformed smoothly under undivided electrolytic cell conditions. Moreover, this electrosynthesis strategy not only avoided the use of chemical oxidants and transition metal catalysts, but also exhibited excellent atom economy.</pubmed_abstract><journal>Chemical science</journal><pubmed_title>Electrochemical oxidative C-H/S-H cross-coupling between enamines and thiophenols with H&lt;sub>2&lt;/sub> evolution.</pubmed_title><pmcid>PMC6419947</pmcid><funding_grant_id>21390402, 21520102003</funding_grant_id><funding_grant_id>2017CFA010</funding_grant_id><pubmed_authors>Lu L</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Peng C</pubmed_authors><pubmed_authors>Cong H</pubmed_authors><pubmed_authors>Chen YH</pubmed_authors><pubmed_authors>Lei A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical oxidative C-H/S-H cross-coupling between enamines and thiophenols with H&lt;sub>2&lt;/sub> evolution.</name><description>Electrochemical oxidative C-H/S-H cross-coupling has been developed to construct the C-S bond in a highly straightforward and efficient manner. Various enamines and (hetero)aryl thiols could be transformed smoothly under undivided electrolytic cell conditions. Moreover, this electrosynthesis strategy not only avoided the use of chemical oxidants and transition metal catalysts, but also exhibited excellent atom economy.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Mar</publication><modification>2026-05-07T10:31:16.227Z</modification><creation>2025-06-01T01:17:45.562Z</creation></dates><accession>S-EPMC6419947</accession><cross_references><pubmed>30996999</pubmed><doi>10.1039/c8sc05143g</doi></cross_references></HashMap>